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Human Molecular Genetics|April 10, 1999
Generation of an approximately 2.4 Mb human X centromere-based minichromosome by targeted telomere-associated chromosome fragmentation in DT40W Mills, R Critcher, C Lee, et al.Human Molecular Genetics|April 10, 1999
Impaired synaptic plasticity in mice carrying the Huntington's disease mutationM T Usdin, P F Shelbourne, R M Myers, et al.Human Molecular Genetics|April 10, 1999
Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7K Tamaki, C A May, Y E Dubrova, et al.Human Molecular Genetics|April 10, 1999
Germline BRCA1 alterations in a population-based series of ovarian cancer casesS A Janezic, A Ziogas, L M Krumroy, et al.Human Molecular Genetics|April 10, 1999
DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in childrenP J Fisher, D Turic, N M Williams, et al.Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.Human Molecular Genetics|October 23, 2003
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseYi-Ju Li, Sofia A Oliveira, Puting Xu, et al.Human Molecular Genetics|October 23, 2003
Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesisLaura Kennedy, Elizabeth Evans, Chiung-Mei Chen, et al.Human Molecular Genetics|October 23, 2003
Phosphorylation influences the translation state of FMRP-associated polyribosomesStephanie Ceman, William T O'Donnell, Matt Reed, et al.Human Molecular Genetics|October 23, 2003
Autophagy regulates the processing of amino terminal huntingtin fragmentsZheng-Hong Qin, Yumei Wang, Kimberly B Kegel, et al.Pageof 1,196